Eupatorium perfoliatum

Manufacturer
Washington Homeopathic Products
Effective date
2023-10-18
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:22:44

Label at a glance#

ProductEupatorium perfoliatum
Active ingredientEUPATORIUM PERFOLIATUM FLOWERING TOP
Label structure8 sections

Indications and uses

To relieve the symptoms of flu-like symptoms.

Dosage and administration

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

EUPATORIUM PERF

USES

OTC - PURPOSE SECTION

To relieve the symptoms of flu-like symptoms.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medicines out of reach of children.

INDICATIONS

INDICATIONS & USAGE SECTION

Indications:

EUPATORIUM PERF   Flu-like symptoms

STOP USE AND ASK DOCTOR

WARNINGS SECTION

If symptoms persist/worsen or if pregnant/nursing, stop use and consult your practitioner.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Adults: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.  Children: Dissolve 3 to 5 under the tongue three times a day or as directed by Lic. Practitioner. Take at greater intervals as condition subsides.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Sucrose/Lactose

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

The OTC potency range of EUPATORIUM PERF is 6x–30x, 3c–30c, 200c, 1m, 10m, 50m, and CM.

Availability is subject to change.

Eupatorium2023Eupatorium2023

All WHP single remedies are made to order; thus, the labels are printed on the same label stock as the orders are filled.

‘Bottle Size’ and ‘Potency’ vary on the label depending on customer choice.

Standard bottle sizes for pellet-form remedies are 2 dram, 4 dram, 1 ounce, 2 ounce, and 4 ounce.

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68428-376-03Eupatorium perfoliatum75 in 1 VIAL, GLASSPELLET754
68428-376-05Eupatorium perfoliatum150 in 1 VIAL, GLASSPELLET1504
68428-376-06Eupatorium perfoliatum1200 in 1 BOTTLE, GLASSPELLET12004
68428-376-11Eupatorium perfoliatum300 in 1 BOTTLE, GLASSPELLET3004
68428-376-12Eupatorium perfoliatum600 in 1 BOTTLE, GLASSPELLET6004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68428-376EUPATORIUM PERFOLIATUM (EUPATORIUM PERFOLIATUM FLOWERING TOP) PELLET [WASHINGTON HOMEOPATHIC PRODUCTS]4Legacy NDC, 5 package rows20231019_ba4e5a44-5b2b-4af8-9a47-b5ce5f994351.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68428-37668428-376-03, 68428-376-05, 68428-376-11, 68428-376-12, 68428-376-06

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0803f98e-7348-2595-e063-6394a90af8ddba4e5a44-5b2b-4af8-9a47-b5ce5f9943512023-10-18WarningsExact identifier
spl id: 0803f98e-7348-2595-e063-6394a90af8dd
spl set id: ba4e5a44-5b2b-4af8-9a47-b5ce5f994351

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.